NO MORE DRIP FOR NOSE COMFORT (Relieves nasal congestion, sinus congestion, rehydrate nasal passages, allergy relief, concentrated lettuce fermentation)

NO MORE DRIP FOR NOSE COMFORT (Relieves nasal congestion, sinus congestion, rehydrate nasal passages, allergy relief, concentrated lettuce fermentation) by

Drug Labeling and Warnings

NO MORE DRIP FOR NOSE COMFORT (Relieves nasal congestion, sinus congestion, rehydrate nasal passages, allergy relief, concentrated lettuce fermentation) by is a Otc medication manufactured, distributed, or labeled by HumanEnos LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NO MORE DRIP FOR NOSE COMFORT (RELIEVES NASAL CONGESTION, SINUS CONGESTION, REHYDRATE NASAL PASSAGES, ALLERGY RELIEF, CONCENTRATED LETTUCE FERMENTATION)- ntric oxide liquid
HumanEnos LLC

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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NO MORE DRIP FOR NOSE COMFORT (Relieves nasal congestion, sinus congestion, rehydrate nasal passages, allergy relief, concentrated lettuce fermentation)

20 ml/ 0.7 oz

KEEP OUT OF THE REACH OF CHILDREN

N:O more Drip Nasal Spray

Warnings

N:O more Drip Nasal Spray

Inactive ingredients:

Lettuce

Active ingredients:

Ntric Oxide

NO MORE DRIP FOR NOSE COMFORT (RELIEVES NASAL CONGESTION, SINUS CONGESTION, REHYDRATE NASAL PASSAGES, ALLERGY RELIEF, CONCENTRATED LETTUCE FERMENTATION)
ntric oxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83202-1469
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
NITRIC OXIDE (UNII: 31C4KY9ESH) (NITRIC OXIDE - UNII:31C4KY9ESH)	NITRIC OXIDE	10 mg in 20 mg

Ingredient Name	Strength
Inactive Ingredients
LETTUCE (UNII: 5PO6NN3RRJ)	1 mg in 20 mg

Product Characteristics
Color	white	Score	score with uneven pieces
Shape	CAPSULE	Size	20mm
Flavor	FRUIT	Imprint Code	capsule
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC: 83202-1469-3	20 mg in 1 CAPSULE; Type 0: Not a Combination Product	02/13/2024	02/12/2025

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		02/13/2024	02/12/2025

Labeler - HumanEnos LLC (695801540)

Name	Address	ID/FEI	Business Operations
Establishment
HumanEnos LLC		695801540	manufacture(83202-1469)

Revised: 2/2024

Document Id: 0f6e3a34-2d0f-de23-e063-6294a90ab08e

Set id: f6196a8c-84aa-20c2-e053-2995a90a41ea

Version: 2

Effective Time: 20240212